US5669051A - Method of electrostatically forming visual image - Google Patents
Method of electrostatically forming visual image Download PDFInfo
- Publication number
- US5669051A US5669051A US08/627,182 US62718296A US5669051A US 5669051 A US5669051 A US 5669051A US 62718296 A US62718296 A US 62718296A US 5669051 A US5669051 A US 5669051A
- Authority
- US
- United States
- Prior art keywords
- magnetic
- permanent magnet
- toner
- magnet member
- carrier
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 238000000034 method Methods 0.000 title claims abstract description 27
- 230000000007 visual effect Effects 0.000 title claims abstract description 15
- 230000005291 magnetic effect Effects 0.000 claims abstract description 93
- 238000012546 transfer Methods 0.000 claims abstract description 14
- 229920005989 resin Polymers 0.000 claims description 44
- 239000011347 resin Substances 0.000 claims description 44
- 239000002245 particle Substances 0.000 claims description 37
- 230000002093 peripheral effect Effects 0.000 claims description 13
- 238000012360 testing method Methods 0.000 description 14
- 239000006229 carbon black Substances 0.000 description 11
- 229910052751 metal Inorganic materials 0.000 description 9
- 239000002184 metal Substances 0.000 description 9
- 230000004907 flux Effects 0.000 description 7
- -1 polyethylenes Polymers 0.000 description 7
- 239000000843 powder Substances 0.000 description 7
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
- 238000011161 development Methods 0.000 description 6
- 239000006247 magnetic powder Substances 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 238000004140 cleaning Methods 0.000 description 5
- 239000011248 coating agent Substances 0.000 description 5
- 238000000576 coating method Methods 0.000 description 5
- 239000000839 emulsion Substances 0.000 description 5
- 239000006249 magnetic particle Substances 0.000 description 5
- 230000005415 magnetization Effects 0.000 description 5
- MWUXSHHQAYIFBG-UHFFFAOYSA-N nitrogen oxide Inorganic materials O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 description 5
- 229920002050 silicone resin Polymers 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 4
- 230000007547 defect Effects 0.000 description 4
- SZVJSHCCFOBDDC-UHFFFAOYSA-N iron(II,III) oxide Inorganic materials O=[Fe]O[Fe]O[Fe]=O SZVJSHCCFOBDDC-UHFFFAOYSA-N 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 229910000859 α-Fe Inorganic materials 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 3
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Natural products C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000004020 conductor Substances 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 150000002739 metals Chemical class 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 229920001225 polyester resin Polymers 0.000 description 3
- 239000004645 polyester resin Substances 0.000 description 3
- 230000001105 regulatory effect Effects 0.000 description 3
- JLIDVCMBCGBIEY-UHFFFAOYSA-N 1-penten-3-one Chemical compound CCC(=O)C=C JLIDVCMBCGBIEY-UHFFFAOYSA-N 0.000 description 2
- ZGHFDIIVVIFNPS-UHFFFAOYSA-N 3-Methyl-3-buten-2-one Chemical compound CC(=C)C(C)=O ZGHFDIIVVIFNPS-UHFFFAOYSA-N 0.000 description 2
- 229910002012 Aerosil® Inorganic materials 0.000 description 2
- 229920000049 Carbon (fiber) Polymers 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- 229920000181 Ethylene propylene rubber Polymers 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- 239000002174 Styrene-butadiene Substances 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 239000004917 carbon fiber Substances 0.000 description 2
- 239000012461 cellulose resin Substances 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000003822 epoxy resin Substances 0.000 description 2
- FJKIXWOMBXYWOQ-UHFFFAOYSA-N ethenoxyethane Chemical compound CCOC=C FJKIXWOMBXYWOQ-UHFFFAOYSA-N 0.000 description 2
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 2
- 230000002209 hydrophobic effect Effects 0.000 description 2
- 238000003384 imaging method Methods 0.000 description 2
- 239000000696 magnetic material Substances 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 229920000647 polyepoxide Polymers 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 230000000717 retained effect Effects 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000011115 styrene butadiene Substances 0.000 description 2
- 229920003048 styrene butadiene rubber Polymers 0.000 description 2
- KTZVZZJJVJQZHV-UHFFFAOYSA-N 1-chloro-4-ethenylbenzene Chemical compound ClC1=CC=C(C=C)C=C1 KTZVZZJJVJQZHV-UHFFFAOYSA-N 0.000 description 1
- OZCMOJQQLBXBKI-UHFFFAOYSA-N 1-ethenoxy-2-methylpropane Chemical compound CC(C)COC=C OZCMOJQQLBXBKI-UHFFFAOYSA-N 0.000 description 1
- CFVWNXQPGQOHRJ-UHFFFAOYSA-N 2-methylpropyl prop-2-enoate Chemical compound CC(C)COC(=O)C=C CFVWNXQPGQOHRJ-UHFFFAOYSA-N 0.000 description 1
- JLBJTVDPSNHSKJ-UHFFFAOYSA-N 4-Methylstyrene Chemical compound CC1=CC=C(C=C)C=C1 JLBJTVDPSNHSKJ-UHFFFAOYSA-N 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- 229910000838 Al alloy Inorganic materials 0.000 description 1
- 229910000906 Bronze Inorganic materials 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- 229910001047 Hard ferrite Inorganic materials 0.000 description 1
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 229910001035 Soft ferrite Inorganic materials 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 239000004809 Teflon Substances 0.000 description 1
- 229920006362 Teflon® Polymers 0.000 description 1
- 229920006311 Urethane elastomer Polymers 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 238000003915 air pollution Methods 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 235000006708 antioxidants Nutrition 0.000 description 1
- 239000000987 azo dye Substances 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- INLLPKCGLOXCIV-UHFFFAOYSA-N bromoethene Chemical compound BrC=C INLLPKCGLOXCIV-UHFFFAOYSA-N 0.000 description 1
- 239000010974 bronze Substances 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 230000001276 controlling effect Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- KUNSUQLRTQLHQQ-UHFFFAOYSA-N copper tin Chemical compound [Cu].[Sn] KUNSUQLRTQLHQQ-UHFFFAOYSA-N 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 230000005684 electric field Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- UIWXSTHGICQLQT-UHFFFAOYSA-N ethenyl propanoate Chemical compound CCC(=O)OC=C UIWXSTHGICQLQT-UHFFFAOYSA-N 0.000 description 1
- 229920006244 ethylene-ethyl acrylate Polymers 0.000 description 1
- 230000005294 ferromagnetic effect Effects 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- XUCNUKMRBVNAPB-UHFFFAOYSA-N fluoroethene Chemical compound FC=C XUCNUKMRBVNAPB-UHFFFAOYSA-N 0.000 description 1
- NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical compound FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 description 1
- SLGWESQGEUXWJQ-UHFFFAOYSA-N formaldehyde;phenol Chemical class O=C.OC1=CC=CC=C1 SLGWESQGEUXWJQ-UHFFFAOYSA-N 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- PBOSTUDLECTMNL-UHFFFAOYSA-N lauryl acrylate Chemical compound CCCCCCCCCCCCOC(=O)C=C PBOSTUDLECTMNL-UHFFFAOYSA-N 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- AWJZTPWDQYFQPQ-UHFFFAOYSA-N methyl 2-chloroprop-2-enoate Chemical compound COC(=O)C(Cl)=C AWJZTPWDQYFQPQ-UHFFFAOYSA-N 0.000 description 1
- XJRBAMWJDBPFIM-UHFFFAOYSA-N methyl vinyl ether Chemical compound COC=C XJRBAMWJDBPFIM-UHFFFAOYSA-N 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- HILCQVNWWOARMT-UHFFFAOYSA-N non-1-en-3-one Chemical compound CCCCCCC(=O)C=C HILCQVNWWOARMT-UHFFFAOYSA-N 0.000 description 1
- ANISOHQJBAQUQP-UHFFFAOYSA-N octyl prop-2-enoate Chemical compound CCCCCCCCOC(=O)C=C ANISOHQJBAQUQP-UHFFFAOYSA-N 0.000 description 1
- UCUUFSAXZMGPGH-UHFFFAOYSA-N penta-1,4-dien-3-one Chemical class C=CC(=O)C=C UCUUFSAXZMGPGH-UHFFFAOYSA-N 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- WRAQQYDMVSCOTE-UHFFFAOYSA-N phenyl prop-2-enoate Chemical compound C=CC(=O)OC1=CC=CC=C1 WRAQQYDMVSCOTE-UHFFFAOYSA-N 0.000 description 1
- 238000007747 plating Methods 0.000 description 1
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920005668 polycarbonate resin Polymers 0.000 description 1
- 239000004431 polycarbonate resin Substances 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 229920001909 styrene-acrylic polymer Polymers 0.000 description 1
- 229920005792 styrene-acrylic resin Polymers 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- KOZCZZVUFDCZGG-UHFFFAOYSA-N vinyl benzoate Chemical compound C=COC(=O)C1=CC=CC=C1 KOZCZZVUFDCZGG-UHFFFAOYSA-N 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Images
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G13/00—Electrographic processes using a charge pattern
- G03G13/06—Developing
- G03G13/08—Developing using a solid developer, e.g. powder developer
- G03G13/09—Developing using a solid developer, e.g. powder developer using magnetic brush
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G9/00—Developers
- G03G9/08—Developers with toner particles
- G03G9/10—Developers with toner particles characterised by carrier particles
- G03G9/107—Developers with toner particles characterised by carrier particles having magnetic components
Definitions
- the present invention relates to a method of electrophotographically producing a visual toner image wherein an electrostatic latent image on a rotating photoconductive drum (image-bearing member) is developed by a magnetic developer attractively retained on the surface of a developer transporting means formed from a cylindrical permanent magnet member.
- an electrophotographic visual image-forming method by which the adhesion of a carrier in the magnetic developer to the surface of the photoconductive drum can be effectively avoided.
- an electrostatic latent image is formed on the surface of a cylindrical photoconductive drum.
- a developing roll composed of a sleeve and a permanent magnet mounted interiorly of the sleeve and rotatably relative to the sleeve is disposed opposite to the photoconductive drum.
- a magnetic developer is magnetically attracted on the surface of the sleeve and transported by the relative rotation of the sleeve and the magnet.
- the magnetic developer transported to a developing zone forms a magnetic brush which brushes the surface of the photoconductive drum to develop the electrostatic latent image to a visual toner image.
- the toner image is transferred onto a recording sheet which is then heated to permanently fix the toner image thereon.
- a corona discharging method in which a high voltage such as DC 5-8 kV is applied to a metal wire to generate corona, is employed to charge the photoconductive surface to a uniform potential and transfer the toner image onto the recording sheet.
- the corona discharge is accompanied with undesired by-products such as ozone, nitrogen oxides (NOx), etc. to cause air pollution due to discomfortable odor, etc.
- the undesired by-products change the properties of the photoconductive surface to reproduce obscure or blurred images.
- the corona wire is stained, the toner images with non-developed portion, undesired toner lines on the background, etc. are produced.
- a recording sheet is applied with a corona charge of the opposite polarity to that of the toner particles in the toner image.
- the charge applied to the recording sheet overcomes the attraction of the latent image to the toner particles and electrostatically pulls them onto the recording sheet. Therefore, the transferring process is considerably affected by an ambient moisture which changes the electrical resistance of the recording sheet. Also, when the resistance of the recording sheet is low, the transfer efficiency of the toner images to the recording sheet is undesirably reduced.
- the corona discharge utilizes only 5-30% of a supplied electric current for charging the photoconductive surface and a recording sheet, and the greater part of the supplied current is lost through a shield plate.
- a charging means and a transferring means utilizing corona discharge are low in the power efficiency. Therefore, a large quantity of power and a high-voltage transformer with high capacity are required for obtaining a desired effect.
- FIG. 1 is a schematic view showing a sleeve-less image forming apparatus employing a brush charging means.
- a magnetic developer 2 mainly comprising a toner and a magnetic carrier is stored in a developer storage 1.
- a cylindrical permanent magnet member 4 is rotatably disposed in the lower portion of the developer storage 1.
- the permanent magnet member 4 has on its exterior circumferential surface a plurality of magnetic poles extending along the axial direction, and at least the surface thereof is made electrically conductive.
- the permanent magnet member 4 is formed from a resin-bonded magnet comprising a ferromagnetic powder and a resin as disclosed in JP-A-57-130407, JP-A-59-905, JP-A-59-226367, etc.
- the surface of the permanent magnet member 4 is made electrically conductive by coating or plating a conductive layer on the surface, or by adding an electrically conductive material during kneading the starting material.
- a semi-conductive permanent magnet member made of a hard ferrite magnet may be also used.
- a photoconductive drum 3 which is rotatable in the direction indicated by an arrow is disposed opposite to the permanent magnet member 4 with a developing gap (g).
- the thickness of the magnetic developer layer magnetically attracted on the surface of the permanent magnet member 4 is regulated by a doctor blade 5 which is attached to an end portion of the developer storage 1 with a doctor gap (t).
- a brush charging means 6, a transfer roll 7, a cleaning means 8 and a blade 9 are disposed around the photoconductive drum 3.
- the magnetic developer 2 attracted on the permanent magnet member 4 is biased with direct current from an electric source (not shown) through the permanent magnet member 4 or the doctor blade 5.
- the surface of the photoconductive drum 3 is brushed with the charging brush of the brush charging means 6 to be charged to a uniform potential.
- the charged portion of the photoconductive drum 3 is exposed to a light image (not shown) to record an electrostatic latent image corresponding to the original information to be reproduced.
- the magnetic developer 2 is attracted on the permanent magnet member 4 and transported to a developing zone defined by the space between the photoconductive drum 3 and the permanent magnet member 4. In the developing zone, a toner in the magnetic developer 2 is deposited on the electrostatic latent image by the electrostatic attraction of the latent image to form a visual toner image on the photoconductive drum 3.
- the visual toner image is transferred to a recording sheet 10 by the transfer roll 7.
- the transferred toner image moves in the direction indicated by an arrow and is fixed to the recording sheet 10 by a fixing means (not shown).
- the toner remaining on the photoconductive drum 3 after transferring step is recovered into the cleaning means 8 by the blade 9 contacting with the surface of the photoconductive drum 3.
- the magnetic carrier in the magnetic developer 2 is likely to adhere to the photoconductive drum 3.
- the adhered carrier passed through the blade 9 causes various drawbacks when reaches the charging brush 6.
- the magnetic carrier is usually electrically conductive, a leak of charge occurs when the magnetic carrier on the photoconductive drum 3 is brought into contact with the charging brush 6. This causes non-uniform charging of the photoconductive surface, generation of loud noise, image defects such as black spots, etc. and, in the extreme case, involves a danger of fires.
- a solution for the above problems may be to tightly and strongly press the blade 9 on to the surface of the photoconductive drum 3 to completely remove the adhered carrier. However, this is likely to damage the photoconductive surface and decreases the life of the photoconductive drum 3. Such problems caused by the adhered carrier on the photoconductive drum 3 becomes more serious in a small-sized image forming apparatus omitting a cleaning means 8.
- an object of the present invention is to provide a method of electrophotographically forming visual images which is free from the problems mentioned above, in particular, capable of avoiding the carrier adhesion to the photoconductive surface thereby producing visual images of high quality.
- a combination of a charging brush, a sleeve-less developing roll (cylindrical permanent magnet member) and a magnetic carrier having a specific volume resistance of particular range can effectively prevent the magnetic carrier from adhering to the photoconductive surface.
- a method of electrostatically forming visual image comprising the steps of (1) charging the surface of a rotating photoconductive drum to a uniform potential by a charging brush; (2) exposing the charged surface of the photoconductive drum to a light image to form an electrostatic latent image; (3) forming a visual toner image on the photoconductive drum by developing the electrostatic latent image in a developing zone with a two-component magnetic developer which is transported to the developing zone by a rotating cylindrical permanent magnet member having on the circumferential surface thereof a plurality of magnetic poles extending along the axial direction, the magnetic developer comprising a magnetic carrier having a specific volume resistance of 10 5 -10 10 ⁇ cm; (4) transferring the toner image to a recording sheet by means of a transfer roll; and (5) fixing the transferred toner image to the recording sheet.
- FIG. 1 is a schematic view showing a sleeve-less image forming apparatus employing a charging means with a charging brush.
- an image forming apparatus as shown in FIG. 1 may be used.
- a photoconductive drum 3 having a photoconductive surface which may be formed from an organic photoconductive material, etc. rotates to a charging zone where the photoconductive surface is charged by a charging brush 6 to a uniform potential, preferably in the range of 400-800 V by means of absolute value.
- the bristle of the charging brush 6 is necessary to be electrically conductive and preferred to have a specific volume resistance of 10 6 ⁇ cm or less.
- the electrically conductive material for the bristle may include carbon fiber, fibers containing therein dispersed electrically conductive particles such as carbon black particles metal powder, etc.
- the charged photoconductive surface rotates to an exposure zone and exposed there by a known exposure unit to a light image corresponding to the original information to be reproduced.
- the photoconductive drum 3 rotates to bring the electrostatic latent image to a developing zone.
- a magnetic developer 2 described in detail below is magnetically attracted on the surface of a permanent magnet member 4 and transported to the developing zone through a doctor blade 5.
- the electrostatic latent image is developed by a contact- or jumping-developing method to form a visual toner image on the photoconductive surface.
- the permanent magnet member 4 may be composed of a ferrite magnet or a resin bonded magnet mainly composed of a magnetic powder and a resin material which may include one or more of ethylene-ethyl acrylate copolymers, polyamides, chlorinated polyethylenes, etc.
- the permanent magnet member 4 may be a roll integrally molded on the outer surface of a shaft 11, or the permanent magnet member 4 and the shaft 11 may be integrally molded from the material described above.
- the permanent magnet member 4 is preferred to have no seam on the exterior circumferential surface thereof to avoid uneven development.
- the surface magnetic flux density decreases with the number of the magnetic pole on the exterior circumferential surface of the permanent magnet member 4, because the N-poles and S-poles are alternatively aligned in the circumferential direction with a small inter-pole pitch.
- a surface magnetic flux density of 50 G or more is preferred to prevent the magnetic developer from scattering, and 1200 G or less is preferred to readily deposit the toner to the latent image on the photoconductive drum 3.
- the preferred range for the surface magnetic flux density is 100-800 G.
- the number of magnetic poles is preferably 8-60 because such a number of magnetic poles generates a surface magnetic flux density of 50-1200 G.
- the magnetic field around the surface of the permanent magnet member 4 decreases smaller with the increase in the number of magnetic poles, the amount of the magnetic developer 2 attracted on the permanent magnet member 4 also becomes smaller. Therefore, the magnetic developer layer on the permanent magnet member 4 becomes wavy or undulated to cause uneven development.
- the permanent magnet member 4 is rotated faster in the case of an increased number of magnetic poles. However, when rotated too fast, the driving torque is unfavorably large and the carrier in the magnetic developer 2 is abraded. On the other hand, when rotated too slowly, images of uneven density are produced.
- the peripheral speed (Vm) of the permanent magnet member 4 is preferably 1 to 10 times, more preferably 2 to 6 times the peripheral speed (Vp) of the photoconductive drum 3.
- the peripheral speed (Vm) is preferably 50-250 mm/sec, more preferably 100-200 mm/sec.
- peripheral speeds (Vm and Vp), the outer diameter of the permanent magnet member 4 and the number of magnetic poles (M) are preferred to be selected so that the value for h (mm) expressed by the following formula:
- the value h means the circumferential length of the photoconductive surface to move during the surface of the permanent magnet member 4 moves inter-pole pitch, namely, the photoconductive surface faces most closely to each magnetic pole every time the photoconductive surface moves a length of h. Since uneven development becomes appreciable when 2 mm or more, the value of h is preferably less than 2 mm, more preferably 1 mm or less.
- the value of h can be made minute by increasing the peripheral speed (Vm) and the number of magnetic poles (M). However, the surface magnetic flux density is reduced when M is too large to result in scattering of the magnetic developer 2, and the problems mentioned above are raised when Vm is too large. Therefore, the value for h is preferably 0.4-1.0 mm in practical developing operations
- a doctor blade 5 is attached to an end portion of a developer storage 1 with or without a gap between the tip thereof and the surface of the permanent magnet member 4 to regulate the thickness of the magnetic developer layer attracted on the permanent magnet member 4.
- the doctor blade may be disposed with no gap so as to contact with or be pressed on the surface of the permanent magnet member 4.
- the magnetic developer 2 on the permanent magnet member 4 is preferred to be biased with direct current, for example, through the permanent magnet member 4.
- the surface of the permanent magnet member 4 is coated with an electrically conductive layer of, for example, a non-magnetic metal such as Cu, SUS, aluminum alloys, etc.
- the doctor blade 5 is preferably made from an electrically conductive material such as metals, etc. to bias the magnetic developer 2 on the permanent magnet member 4 therethrough.
- a relatively low frequency alternating current of 20 kHz or less, preferably 10 kHz or less may be superimposed to direct current.
- the peak-to-peak value (Vp-p) is preferably 100-2000 V, more preferably 200-1200 V.
- the visual toner image is moved to a transfer zone where the toner image is transferred to a recording sheet 10 by a transfer roll 7.
- the transfer roll 7 may comprise a metal shaft 12 around which an electrically conductive elastic layer of urethane rubber, butadiene rubber, ethylene-propylene rubber, etc. is coated.
- the elastic layer is preferred to have a specific volume resistance of 10 6 ⁇ cm or less.
- the toner remaining on the photoconductive drum after transferring the toner image to the recording sheet may be recovered by a cleaning means 8 having a blade 9 contacting the surface of the photoconductive drum 3.
- the cleaning means 8 may be omitted to minimize the apparatus.
- two-component magnetic developer comprising a magnetic toner and a magnetic carrier (10-90 weight % toner concentration) or comprising a non-magnetic toner and a magnetic carrier (5-60 weight % toner concentration) may be used.
- a magnetic particle such as iron powder, ferrite powder, magnetite powder, resin bonded particle comprising a resin containing a dispersed magnetic powder, etc.
- a flat carrier is preferable rather than a spherical carrier because the toner obtains a sufficient amount of triboelectric charge.
- the carrier is preferred to have an average particle size of 10-150 ⁇ m, preferably 10-50 ⁇ m, a specific volume resistance of 10 5 -10 10 ⁇ cm, preferably 10 6 -10 9 ⁇ cm, and a magnetization ( ⁇ 1000 ) of 30 emu/g or more, preferably 60 emu/g or more at 1000 Oe magnetic field.
- An average particle size exceeding 150 ⁇ m is not desirable because the carrier fails to give the toner a sufficient triboelectric charge.
- the average particle size is less than 10 ⁇ m, the magnetization ( ⁇ 1000) is lower than 30 emu/g, or the specific volume resistance is lower than 10 5 ⁇ cm, the carrier is likely to adhere to the photoconductive drum 3, which results in deterioration of image quality, occurrence of leak at the charging brush 6, difficulty in providing the toner with a constant amount of triboelectric charge, etc.
- the specific volume resistance exceeds 10 10 ⁇ cm, the magnetic developer 2 on the permanent magnet member is hard to be biased to result in deterioration of image quality.
- the specific volume resistance is regulated within the range of 10 5 -10 10 ⁇ cm, for example, by coating the surface of the carrier with a resin.
- the resin coating thus formed on the carrier may optionally contain therein and/or on the surface thereof an additive such as electrically conductive particles such as carbon black powder, metal powder, etc., charge controlling agent, anti-oxidant, etc.
- the electrically conductive particles may be internally added in the resin layer in an amount about 5-15 weight % based on the total amount of the resin layer, while about 0.5-5 weight parts based on 100 weight parts of the carrier core when externally added to the resin layer.
- Suitable materials for the resin layers may include homopolymers or copolymers of styrene compound such as p-chlorostyrene, methylstyrene, etc.; vinyl halides such as vinyl chloride, vinyl bromide, vinyl fluoride, etc.; vinyl esters such as vinyl acetate, vinyl propionate, vinyl benzoate, etc.; esters of ⁇ , ⁇ -unsaturated aliphatic monocarboxylic acid such as methyl acrylate, ethyl acrylate, butyl acrylate, isobutyl acrylate, dodecyl acrylate, n-octyl acrylate, 3-chloroethyl acrylate, phenyl acrylate, methyl ⁇ -chloroacrylate, butyl methacrylate, etc.; nitriles such as acrylonitrile, methacrylonitrile, etc.; amides such as acrylamide, etc.; vinyl ethers such as
- resins such as epoxy resins, silicone resins, rosin-modified phenol-formaldehyde resins, cellulose resins, polyether resins, polyvinyl butyral resins, polyester resins, styrene-butadiene resins, polyurethane resins, polycarbonate resins, fluorocarbon resins such as tetrafluoroethylene, etc. may be also usable. These resin materials may be used alone or in combination. Among them, styrene-acrylic resins, silicone resins, epoxy resins, styrene-butadiene resins, cellulose resins, etc. are particularly preferable.
- the carrier is coated with resins, for example, according to the following method.
- the resin material is dissolved in an adequate solvent such as benzene, toluene, xylene, methyl ethyl ketone, tetrahydrofuran, chloroform, hexane, etc., to produce a resin solution or emulsion.
- an electrically conductive particle is further added to the resin solution or emulsion.
- the resin solution or emulsion thus prepared is sprayed onto the surface of the carrier to form uniform resin layer thereon.
- the carrier is preferably maintained in a fluidized state desirably by employing a spray dryer or a fluidized bed.
- the solution is sprayed at about 200° C. or lower, preferably at about 100°-150° C., to rapidly remove a solvent from the resultant resin layer.
- the resin emulsion the emulsion is sprayed at a temperature from room temperature to 100° C. to adhere the fused resin to the surface of the carrier.
- the carrier is coated with the resin in an amount of 0.2-10 weight parts, preferably 1-5 weight parts based on 100 weight parts of the carrier.
- the carrier may be a mixture of two or more of the above magnetic particles.
- a large-sized magnetic particle having an average particle size of 60-120 ⁇ m may be mixed with a small-sized magnetic particle having an average particle size of 10-50 ⁇ m or a small-sized bonded magnetic particle having an average particle size of 10-50 ⁇ m.
- the mixing ratio may be determined depending upon the particle size, magnetic properties, etc., in particular determined so that the average particle size of mixed carrier falls within the above range of 10-150 ⁇ m.
- the toner may be either magnetic or non-magnetic.
- the toner is preferred to be electrically insulating, i.e., have a specific volume resistance of 10 14 ⁇ cm or more.
- a toner which can be easily triboelectrically charged easily reaches a triboelectric charge of 10 ⁇ C/g or more (absolute value)) by the friction with the carrier and/or the doctor blade, etc. is preferable.
- the volume average particle size of the toner may be 5-10 ⁇ m, preferably 5-8 ⁇ m.
- the toner composition may be the same as those known in the art.
- the toner comprises a binder resin (styrene-acrylic copolymer, polyester resin, etc.) and a colorant (carbon black, etc., however not needed to be used when magnetite is used for a magnetic powder component) as the essential component, and a magnetic powder (magnetite, soft ferrite, etc.), a charge-controlling agent (nigrosine, metal-containing azo dye, etc.), a lubricant (polyolefin, etc.) and a mobility improver (hydrophobic silica) as the optional component.
- a binder resin styrene-acrylic copolymer, polyester resin, etc.
- a colorant carbon black, etc., however not needed to be used when magnetite is used for a magnetic powder component
- a magnetic powder magnetite, soft ferrite, etc.
- a charge-controlling agent nigrosine, metal-containing azo dye
- the content thereof in the toner is preferably 70 weight % or less because a content higher than 70 weight % results in defective fixing.
- the content of the magnetic powder is preferably 10-60 weight %, more preferably 20-50 weight %.
- a color toner may be also produced by suitably selecting the colorant.
- the magnetization and the volume-average particle size of the toner were measured by a vibrating magnetometer (VSM-3 manufactured by Toei Kogyo K.K.) and a particle size analyzer (Coulter Counter Model TA-II manufactured by Coulter Electronics Co.), respectively.
- the weight-average particle size of the carrier was calculated from a particle size distribution obtained by a multi-sieve shaking machine.
- the specific volume resistance was determined as follows. An appropriate amount (about 10 mg) of the toner or carrier was charged into a dial-gauge type cylinder made of Teflon (trade name) and having an inner diameter of 3.05 mm. The sample was exposed to an electric field of D.C. 100 V/cm (magnetic carrier) or D.C. 4000 V/cm (toner) under a load of 0.1 kgf to measure an electric resistance using an insulation-resistance tester (4329 manufactured by Yokogawa-Hewlett-Packard, Ltd.). The triboelectric charge of the toner was determined as follows.
- a magnetic developer having a toner content of 5 weight % was mixed well, and blown at a blowing pressure of 1.0 kgf/cm 2 .
- the triboelectric charge of the toner thus treated was measured by using a blow-off powder electric charge measuring apparatus (TB-200 manufactured by Toshiba Chemical Co. Ltd.).
- a magnetic toner having an average particle size of 10 ⁇ m and a particle size distribution of 4 to 16 ⁇ m was prepared as follows.
- the magnetic toner had a specific volume resistance of 10 15 ⁇ cm and a triboelectric charge of -23 ⁇ C/g.
- the carrier core flat iron powder having an average particles size of 30 ⁇ m, a particle size distribution of 10-50 ⁇ m, and a magnetization ( ⁇ 1000 ) of 120 emu/g was used.
- the carrier was coated with a silicone resin to prepare each resin-coated carrier.
- a resin-coated carrier of relatively high specific volume resistance was prepared by changing the coating amount of silicone resin, while by changing the addition amount (internal addition and external addition) of carbon black (#600 manufactured by Mitsubishi Chemical Industries) as the electrically conductive particle to attain a relatively low specific volume resistance.
- the magnetic toner and the resin-coated magnetic carrier thus produce was mixed in a predetermined ratio to prepare magnetic developers of different toner concentrations.
- the developing properties of each of the magnetic developers were tested by continuous development of 1000 sheets of A4 size papers.
- the operating conditions employed were as follows. Initially, the OPC surface of the photoconductive drum 3 rotating clockwise at a peripheral speed of 30 mm/sec was uniformly charged to -700 V.
- the permanent magnet member 4 which was formed from a 16-pole ferrite magnet (YBM-3 manufactured by Hitachi Metals, Ltd.) having 20 mm outer diameter and 500 G of surface magnetic flux density, was rotated counterclockwise at a peripheral speed of 147 mm/sec.
- the developing gap (g) and the doctor gap (t) were 0.4 mm and 0.3 mm respectively.
- the magnetic developer on the permanent magnet member 4 was biased to -550 V with direct current through the doctor blade 5.
- the charging brush 6 was formed by setting a plurality of carbon fiber bristles having a specific volume resistance of 10 5 ⁇ cm into a substrate of SUS304. The length of bristles was 10 min.
- the transfer roll 7 having an outer diameter of 20 mm was produced by coating around a shaft made Of SUS304 with an ethylene-propylene rubber layer having a hardness (Hs) of 80° and a thickness of 2 mm and pressed against the photoconductive drum 3.
- a non-magnetic toner having an average particle size of 8.5 ⁇ m and a particle size distribution of 3-15 ⁇ m was prepared in the same manner as in Example 1 except for using the following starting mixture.
- polyester resin (KTR2150 manufactured by Kao Corporation)
- the non-magnetic toner thus prepared had a volume specific resistance of 5 ⁇ 10 14 ⁇ cm and a triboelectric charge of -29 ⁇ C/g.
- the carrier flat iron powder having an average particles size of 50 ⁇ m, a particle size distribution of 10-70 ⁇ m, and a magnetization ( ⁇ 1000 ) of 120 emu/g was used.
- the carrier was coated with a silicone resin to prepare each resin-coated carrier having a desired specific volume resistance in the same manner as in Example 1.
- the image forming tests (continuous development of 1000 sheets of A4 size papers) were carried out under the following operating conditions. Initially, the OPC surface of the photoconductive drum 3 rotating clockwise at a peripheral speed of 30 mm/sec was uniformly charged to -650 V.
- the permanent magnet member 4 which was formed from a 32-pole ferrite magnet (YBM-3 manufactured by Hitachi Metals, Ltd.) having 20 mm outer diameter and 350 G of surface magnetic flux density, was rotated counterclockwise at a peripheral speed of 74 mm/sec.
- the developing gap (g) and the doctor gap (t) were 0.4 mm and 0.25 mm, respectively.
- the magnetic developer on the permanent magnet member 4 was biased to -500 V with direct current through the doctor blade 5.
- the same charging brush and the transfer roll as employed in Example 1 were used.
- the developing unit and the electrophotographic recording apparatus can be miniaturized.
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Dry Development In Electrophotography (AREA)
- Developing Agents For Electrophotography (AREA)
- Magnetic Brush Developing In Electrophotography (AREA)
Abstract
A method in which a photoconductive surface is charged to a uniform potential by a charging brush and a two-component magnetic developer is directly attracted on the surfaced of a sleeve-less developing roll formed from a permanent magnet member and transported by the rotation of the permanent magnet member. An electrostatic latent image is developed with the transported magnetic developer in a developing zone to form a visual toner image on the photoconductive drum. The toner image is transferred to a recording sheet by a transfer roll and permanently fixed thereon by a suitable fixing means. The specific volume resistance of the magnetic carrier is restricted to a particular range to prevent the magnetic carrier from adhering to the photoconductive surface.
Description
The present invention relates to a method of electrophotographically producing a visual toner image wherein an electrostatic latent image on a rotating photoconductive drum (image-bearing member) is developed by a magnetic developer attractively retained on the surface of a developer transporting means formed from a cylindrical permanent magnet member. In particular, an electrophotographic visual image-forming method by which the adhesion of a carrier in the magnetic developer to the surface of the photoconductive drum can be effectively avoided.
In a known electrophotographic imaging process and electrostatic recording process utilized in printers, facsimile machines, etc., an electrostatic latent image is formed on the surface of a cylindrical photoconductive drum. A developing roll composed of a sleeve and a permanent magnet mounted interiorly of the sleeve and rotatably relative to the sleeve is disposed opposite to the photoconductive drum. A magnetic developer is magnetically attracted on the surface of the sleeve and transported by the relative rotation of the sleeve and the magnet. The magnetic developer transported to a developing zone forms a magnetic brush which brushes the surface of the photoconductive drum to develop the electrostatic latent image to a visual toner image. The toner image is transferred onto a recording sheet which is then heated to permanently fix the toner image thereon.
In the conventional image forming apparatus, a corona discharging method, in which a high voltage such as DC 5-8 kV is applied to a metal wire to generate corona, is employed to charge the photoconductive surface to a uniform potential and transfer the toner image onto the recording sheet. However, the corona discharge is accompanied with undesired by-products such as ozone, nitrogen oxides (NOx), etc. to cause air pollution due to discomfortable odor, etc. The undesired by-products change the properties of the photoconductive surface to reproduce obscure or blurred images. Further, when the corona wire is stained, the toner images with non-developed portion, undesired toner lines on the background, etc. are produced.
In the corona transfer, a recording sheet is applied with a corona charge of the opposite polarity to that of the toner particles in the toner image. The charge applied to the recording sheet overcomes the attraction of the latent image to the toner particles and electrostatically pulls them onto the recording sheet. Therefore, the transferring process is considerably affected by an ambient moisture which changes the electrical resistance of the recording sheet. Also, when the resistance of the recording sheet is low, the transfer efficiency of the toner images to the recording sheet is undesirably reduced.
The corona discharge utilizes only 5-30% of a supplied electric current for charging the photoconductive surface and a recording sheet, and the greater part of the supplied current is lost through a shield plate. Thus, a charging means and a transferring means utilizing corona discharge are low in the power efficiency. Therefore, a large quantity of power and a high-voltage transformer with high capacity are required for obtaining a desired effect.
To eliminate the above problems in corona discharge, an image forming method employing a brush charging means and a roll transferring means have been proposed.
Further, a requirement to develop small-sized imaging machines has been recently increased. To meet the increasing requirement, it is important to minimize the developing parts. As a proposal realizing the minimization, a developing roll with no sleeve has been proposed to attractively retain magnetic developer on the permanent magnet surface directly and transport the retained magnetic developer to the developing zone by the rotation of the permanent magnet only (JP-A-62-201463).
FIG. 1 is a schematic view showing a sleeve-less image forming apparatus employing a brush charging means. In FIG. 1, a magnetic developer 2 mainly comprising a toner and a magnetic carrier is stored in a developer storage 1. A cylindrical permanent magnet member 4 is rotatably disposed in the lower portion of the developer storage 1. The permanent magnet member 4 has on its exterior circumferential surface a plurality of magnetic poles extending along the axial direction, and at least the surface thereof is made electrically conductive.
The permanent magnet member 4 is formed from a resin-bonded magnet comprising a ferromagnetic powder and a resin as disclosed in JP-A-57-130407, JP-A-59-905, JP-A-59-226367, etc. The surface of the permanent magnet member 4 is made electrically conductive by coating or plating a conductive layer on the surface, or by adding an electrically conductive material during kneading the starting material. A semi-conductive permanent magnet member made of a hard ferrite magnet may be also used.
A photoconductive drum 3 which is rotatable in the direction indicated by an arrow is disposed opposite to the permanent magnet member 4 with a developing gap (g). The thickness of the magnetic developer layer magnetically attracted on the surface of the permanent magnet member 4 is regulated by a doctor blade 5 which is attached to an end portion of the developer storage 1 with a doctor gap (t). A brush charging means 6, a transfer roll 7, a cleaning means 8 and a blade 9 are disposed around the photoconductive drum 3. The magnetic developer 2 attracted on the permanent magnet member 4 is biased with direct current from an electric source (not shown) through the permanent magnet member 4 or the doctor blade 5.
Upon rotating each of the photoconductive drum 3, permanent magnet member 4 and transfer roll 7 in the direction indicated by an arrow, the surface of the photoconductive drum 3 is brushed with the charging brush of the brush charging means 6 to be charged to a uniform potential. The charged portion of the photoconductive drum 3 is exposed to a light image (not shown) to record an electrostatic latent image corresponding to the original information to be reproduced. Separately, the magnetic developer 2 is attracted on the permanent magnet member 4 and transported to a developing zone defined by the space between the photoconductive drum 3 and the permanent magnet member 4. In the developing zone, a toner in the magnetic developer 2 is deposited on the electrostatic latent image by the electrostatic attraction of the latent image to form a visual toner image on the photoconductive drum 3.
The visual toner image is transferred to a recording sheet 10 by the transfer roll 7. The transferred toner image moves in the direction indicated by an arrow and is fixed to the recording sheet 10 by a fixing means (not shown). The toner remaining on the photoconductive drum 3 after transferring step is recovered into the cleaning means 8 by the blade 9 contacting with the surface of the photoconductive drum 3.
However, In the above conventional image forming method, the magnetic carrier in the magnetic developer 2 is likely to adhere to the photoconductive drum 3. The adhered carrier passed through the blade 9 causes various drawbacks when reaches the charging brush 6. For example, since the magnetic carrier is usually electrically conductive, a leak of charge occurs when the magnetic carrier on the photoconductive drum 3 is brought into contact with the charging brush 6. This causes non-uniform charging of the photoconductive surface, generation of loud noise, image defects such as black spots, etc. and, in the extreme case, involves a danger of fires.
A solution for the above problems may be to tightly and strongly press the blade 9 on to the surface of the photoconductive drum 3 to completely remove the adhered carrier. However, this is likely to damage the photoconductive surface and decreases the life of the photoconductive drum 3. Such problems caused by the adhered carrier on the photoconductive drum 3 becomes more serious in a small-sized image forming apparatus omitting a cleaning means 8.
Accordingly, an object of the present invention is to provide a method of electrophotographically forming visual images which is free from the problems mentioned above, in particular, capable of avoiding the carrier adhesion to the photoconductive surface thereby producing visual images of high quality.
As a result of the intense research in view of the above objects, the inventors have found that a combination of a charging brush, a sleeve-less developing roll (cylindrical permanent magnet member) and a magnetic carrier having a specific volume resistance of particular range can effectively prevent the magnetic carrier from adhering to the photoconductive surface.
Thus, in an aspect of the present invention, there is provided a method of electrostatically forming visual image, comprising the steps of (1) charging the surface of a rotating photoconductive drum to a uniform potential by a charging brush; (2) exposing the charged surface of the photoconductive drum to a light image to form an electrostatic latent image; (3) forming a visual toner image on the photoconductive drum by developing the electrostatic latent image in a developing zone with a two-component magnetic developer which is transported to the developing zone by a rotating cylindrical permanent magnet member having on the circumferential surface thereof a plurality of magnetic poles extending along the axial direction, the magnetic developer comprising a magnetic carrier having a specific volume resistance of 105 -1010 Ω·cm; (4) transferring the toner image to a recording sheet by means of a transfer roll; and (5) fixing the transferred toner image to the recording sheet.
FIG. 1 is a schematic view showing a sleeve-less image forming apparatus employing a charging means with a charging brush.
In the image forming method of the present invention, an image forming apparatus as shown in FIG. 1 may be used.
Initially, a photoconductive drum 3 having a photoconductive surface which may be formed from an organic photoconductive material, etc. rotates to a charging zone where the photoconductive surface is charged by a charging brush 6 to a uniform potential, preferably in the range of 400-800 V by means of absolute value. The bristle of the charging brush 6 is necessary to be electrically conductive and preferred to have a specific volume resistance of 106 ω·cm or less. The electrically conductive material for the bristle may include carbon fiber, fibers containing therein dispersed electrically conductive particles such as carbon black particles metal powder, etc.
Next, the charged photoconductive surface rotates to an exposure zone and exposed there by a known exposure unit to a light image corresponding to the original information to be reproduced. Subsequent to the recording of the electrostatic latent image on the photoconductive surface, the photoconductive drum 3 rotates to bring the electrostatic latent image to a developing zone.
Separately, a magnetic developer 2 described in detail below is magnetically attracted on the surface of a permanent magnet member 4 and transported to the developing zone through a doctor blade 5. In the developing zone, the electrostatic latent image is developed by a contact- or jumping-developing method to form a visual toner image on the photoconductive surface.
The permanent magnet member 4 may be composed of a ferrite magnet or a resin bonded magnet mainly composed of a magnetic powder and a resin material which may include one or more of ethylene-ethyl acrylate copolymers, polyamides, chlorinated polyethylenes, etc. The permanent magnet member 4 may be a roll integrally molded on the outer surface of a shaft 11, or the permanent magnet member 4 and the shaft 11 may be integrally molded from the material described above. The permanent magnet member 4 is preferred to have no seam on the exterior circumferential surface thereof to avoid uneven development.
The surface magnetic flux density decreases with the number of the magnetic pole on the exterior circumferential surface of the permanent magnet member 4, because the N-poles and S-poles are alternatively aligned in the circumferential direction with a small inter-pole pitch. A surface magnetic flux density of 50 G or more is preferred to prevent the magnetic developer from scattering, and 1200 G or less is preferred to readily deposit the toner to the latent image on the photoconductive drum 3. The preferred range for the surface magnetic flux density is 100-800 G. The number of magnetic poles is preferably 8-60 because such a number of magnetic poles generates a surface magnetic flux density of 50-1200 G.
Since the magnetic field around the surface of the permanent magnet member 4 decreases smaller with the increase in the number of magnetic poles, the amount of the magnetic developer 2 attracted on the permanent magnet member 4 also becomes smaller. Therefore, the magnetic developer layer on the permanent magnet member 4 becomes wavy or undulated to cause uneven development. To eliminate this problem, the permanent magnet member 4 is rotated faster in the case of an increased number of magnetic poles. However, when rotated too fast, the driving torque is unfavorably large and the carrier in the magnetic developer 2 is abraded. On the other hand, when rotated too slowly, images of uneven density are produced. In view of the above, the peripheral speed (Vm) of the permanent magnet member 4 is preferably 1 to 10 times, more preferably 2 to 6 times the peripheral speed (Vp) of the photoconductive drum 3. The peripheral speed (Vm) is preferably 50-250 mm/sec, more preferably 100-200 mm/sec.
Further, the peripheral speeds (Vm and Vp), the outer diameter of the permanent magnet member 4 and the number of magnetic poles (M) are preferred to be selected so that the value for h (mm) expressed by the following formula:
h=πD·Vp/M·Vm
is less than 2 (mm). The value h means the circumferential length of the photoconductive surface to move during the surface of the permanent magnet member 4 moves inter-pole pitch, namely, the photoconductive surface faces most closely to each magnetic pole every time the photoconductive surface moves a length of h. Since uneven development becomes appreciable when 2 mm or more, the value of h is preferably less than 2 mm, more preferably 1 mm or less. The value of h can be made minute by increasing the peripheral speed (Vm) and the number of magnetic poles (M). However, the surface magnetic flux density is reduced when M is too large to result in scattering of the magnetic developer 2, and the problems mentioned above are raised when Vm is too large. Therefore, the value for h is preferably 0.4-1.0 mm in practical developing operations
A doctor blade 5 is attached to an end portion of a developer storage 1 with or without a gap between the tip thereof and the surface of the permanent magnet member 4 to regulate the thickness of the magnetic developer layer attracted on the permanent magnet member 4. The doctor gap (t) is preferably 0.1-0.4 mm and the developing gap (g) is selected so as to satisfy the formula: g-t=0-0.2 mm. When a flexible and elastic doctor blade made of magnetic material such as SK steel, etc. or non-magnetic material such as SUS304, phosphor bronze, etc. is used, the doctor blade may be disposed with no gap so as to contact with or be pressed on the surface of the permanent magnet member 4.
The magnetic developer 2 on the permanent magnet member 4 is preferred to be biased with direct current, for example, through the permanent magnet member 4. For this purpose, the surface of the permanent magnet member 4 is coated with an electrically conductive layer of, for example, a non-magnetic metal such as Cu, SUS, aluminum alloys, etc. When the permanent magnet member 4 is semi-conductive or electrically insulating, the doctor blade 5 is preferably made from an electrically conductive material such as metals, etc. to bias the magnetic developer 2 on the permanent magnet member 4 therethrough. A relatively low frequency alternating current of 20 kHz or less, preferably 10 kHz or less may be superimposed to direct current. The peak-to-peak value (Vp-p) is preferably 100-2000 V, more preferably 200-1200 V.
After development, the visual toner image is moved to a transfer zone where the toner image is transferred to a recording sheet 10 by a transfer roll 7. The transfer roll 7 may comprise a metal shaft 12 around which an electrically conductive elastic layer of urethane rubber, butadiene rubber, ethylene-propylene rubber, etc. is coated. The elastic layer is preferred to have a specific volume resistance of 106 Ω·cm or less. Then, the sheet is moved to a fixing zone where the transferred image is permanently fixed on the sheet by a known fixing means.
The toner remaining on the photoconductive drum after transferring the toner image to the recording sheet may be recovered by a cleaning means 8 having a blade 9 contacting the surface of the photoconductive drum 3. However, since the carrier adhesion to the photoconductive drum 3 is effectively avoided in the method of the present invention, the cleaning means 8 may be omitted to minimize the apparatus.
In the method of the present invention, two-component magnetic developer comprising a magnetic toner and a magnetic carrier (10-90 weight % toner concentration) or comprising a non-magnetic toner and a magnetic carrier (5-60 weight % toner concentration) may be used.
As the carrier, a magnetic particle such as iron powder, ferrite powder, magnetite powder, resin bonded particle comprising a resin containing a dispersed magnetic powder, etc. may be used. With respect to the shape of the carrier, a flat carrier is preferable rather than a spherical carrier because the toner obtains a sufficient amount of triboelectric charge. The carrier is preferred to have an average particle size of 10-150 μm, preferably 10-50 μm, a specific volume resistance of 105 -1010 Ω·cm, preferably 106 -109 Ω·cm, and a magnetization (σ1000) of 30 emu/g or more, preferably 60 emu/g or more at 1000 Oe magnetic field. An average particle size exceeding 150 μm is not desirable because the carrier fails to give the toner a sufficient triboelectric charge. When the average particle size is less than 10 μm, the magnetization (σ1000) is lower than 30 emu/g, or the specific volume resistance is lower than 105 Ω·cm, the carrier is likely to adhere to the photoconductive drum 3, which results in deterioration of image quality, occurrence of leak at the charging brush 6, difficulty in providing the toner with a constant amount of triboelectric charge, etc. When the specific volume resistance exceeds 1010 Ω·cm, the magnetic developer 2 on the permanent magnet member is hard to be biased to result in deterioration of image quality.
The specific volume resistance is regulated within the range of 105 -1010 Ω·cm, for example, by coating the surface of the carrier with a resin. The resin coating thus formed on the carrier may optionally contain therein and/or on the surface thereof an additive such as electrically conductive particles such as carbon black powder, metal powder, etc., charge controlling agent, anti-oxidant, etc. For example, the electrically conductive particles may be internally added in the resin layer in an amount about 5-15 weight % based on the total amount of the resin layer, while about 0.5-5 weight parts based on 100 weight parts of the carrier core when externally added to the resin layer.
Suitable materials for the resin layers may include homopolymers or copolymers of styrene compound such as p-chlorostyrene, methylstyrene, etc.; vinyl halides such as vinyl chloride, vinyl bromide, vinyl fluoride, etc.; vinyl esters such as vinyl acetate, vinyl propionate, vinyl benzoate, etc.; esters of α,β-unsaturated aliphatic monocarboxylic acid such as methyl acrylate, ethyl acrylate, butyl acrylate, isobutyl acrylate, dodecyl acrylate, n-octyl acrylate, 3-chloroethyl acrylate, phenyl acrylate, methyl α-chloroacrylate, butyl methacrylate, etc.; nitriles such as acrylonitrile, methacrylonitrile, etc.; amides such as acrylamide, etc.; vinyl ethers such as vinyl methyl ether, vinyl isobutyl ether, vinyl ethyl ether, etc.; vinyl ketones such as vinyl ethyl ketone, vinyl hexyl ketone, methyl isopropenyl ketone, etc. Other resins such as epoxy resins, silicone resins, rosin-modified phenol-formaldehyde resins, cellulose resins, polyether resins, polyvinyl butyral resins, polyester resins, styrene-butadiene resins, polyurethane resins, polycarbonate resins, fluorocarbon resins such as tetrafluoroethylene, etc. may be also usable. These resin materials may be used alone or in combination. Among them, styrene-acrylic resins, silicone resins, epoxy resins, styrene-butadiene resins, cellulose resins, etc. are particularly preferable.
The carrier is coated with resins, for example, according to the following method. First, the resin material is dissolved in an adequate solvent such as benzene, toluene, xylene, methyl ethyl ketone, tetrahydrofuran, chloroform, hexane, etc., to produce a resin solution or emulsion. If a relatively low specific volume resistance is desired, an electrically conductive particle is further added to the resin solution or emulsion. The resin solution or emulsion thus prepared is sprayed onto the surface of the carrier to form uniform resin layer thereon. To obtain uniform resin layer, the carrier is preferably maintained in a fluidized state desirably by employing a spray dryer or a fluidized bed. In the case of the resin solution, the solution is sprayed at about 200° C. or lower, preferably at about 100°-150° C., to rapidly remove a solvent from the resultant resin layer. On the other hand, in the case of the resin emulsion, the emulsion is sprayed at a temperature from room temperature to 100° C. to adhere the fused resin to the surface of the carrier. The carrier is coated with the resin in an amount of 0.2-10 weight parts, preferably 1-5 weight parts based on 100 weight parts of the carrier.
The carrier may be a mixture of two or more of the above magnetic particles. For example, a large-sized magnetic particle having an average particle size of 60-120 μm may be mixed with a small-sized magnetic particle having an average particle size of 10-50 μm or a small-sized bonded magnetic particle having an average particle size of 10-50 μm. The mixing ratio may be determined depending upon the particle size, magnetic properties, etc., in particular determined so that the average particle size of mixed carrier falls within the above range of 10-150 μm.
The toner may be either magnetic or non-magnetic. In view of high transferring efficiency, the toner is preferred to be electrically insulating, i.e., have a specific volume resistance of 1014 Ω·cm or more. Also, a toner which can be easily triboelectrically charged (easily reaches a triboelectric charge of 10 μC/g or more (absolute value)) by the friction with the carrier and/or the doctor blade, etc. is preferable. The volume average particle size of the toner may be 5-10 μm, preferably 5-8 μm.
The toner composition may be the same as those known in the art. Generally, the toner comprises a binder resin (styrene-acrylic copolymer, polyester resin, etc.) and a colorant (carbon black, etc., however not needed to be used when magnetite is used for a magnetic powder component) as the essential component, and a magnetic powder (magnetite, soft ferrite, etc.), a charge-controlling agent (nigrosine, metal-containing azo dye, etc.), a lubricant (polyolefin, etc.) and a mobility improver (hydrophobic silica) as the optional component. When the magnetic powder is used, the content thereof in the toner is preferably 70 weight % or less because a content higher than 70 weight % results in defective fixing. The content of the magnetic powder is preferably 10-60 weight %, more preferably 20-50 weight %. A color toner may be also produced by suitably selecting the colorant.
In the present invention, the magnetization and the volume-average particle size of the toner were measured by a vibrating magnetometer (VSM-3 manufactured by Toei Kogyo K.K.) and a particle size analyzer (Coulter Counter Model TA-II manufactured by Coulter Electronics Co.), respectively. The weight-average particle size of the carrier was calculated from a particle size distribution obtained by a multi-sieve shaking machine.
The specific volume resistance was determined as follows. An appropriate amount (about 10 mg) of the toner or carrier was charged into a dial-gauge type cylinder made of Teflon (trade name) and having an inner diameter of 3.05 mm. The sample was exposed to an electric field of D.C. 100 V/cm (magnetic carrier) or D.C. 4000 V/cm (toner) under a load of 0.1 kgf to measure an electric resistance using an insulation-resistance tester (4329 manufactured by Yokogawa-Hewlett-Packard, Ltd.). The triboelectric charge of the toner was determined as follows. A magnetic developer having a toner content of 5 weight % was mixed well, and blown at a blowing pressure of 1.0 kgf/cm2. The triboelectric charge of the toner thus treated was measured by using a blow-off powder electric charge measuring apparatus (TB-200 manufactured by Toshiba Chemical Co. Ltd.).
The present invention will be further described while referring to the following Examples which should be considered to illustrate various preferred embodiments of the present invention.
A magnetic toner having an average particle size of 10 μm and a particle size distribution of 4 to 16 μm was prepared as follows. A starting mixture consisting, by weight part, of:
45 parts of styrene/n-butyl methacrylate copolymer
(weight-average molecular weight (Mw)=21×104, number-average molecular weight (Mn)=1.6×104),
50 parts of magnetite (EPT500 manufactured by Toda kogyo K.K.),
3 parts of polypropylene (TP32 manufactured by Sanyo Chemical Industries, Ltd.), and
2 part of a negatively chargeable charge-controlling agent (Bontron E-81 manufactured by Orient Chemical Industries)
was kneaded under heating, solidified by cooling, pulverized and classified to obtain a particle having an average particle size of 9 μm. The particle thus obtained was mixed with 0.5 parts by weight of hydrophobic silica (Aerosil R972 manufactured by Nippon Aerosil K.K.), thereby producing a negatively chargeable magnetic toner. The magnetic toner had a specific volume resistance of 1015 Ω·cm and a triboelectric charge of -23 μC/g.
As the carrier core, flat iron powder having an average particles size of 30 μm, a particle size distribution of 10-50 μm, and a magnetization (σ1000) of 120 emu/g was used. The carrier was coated with a silicone resin to prepare each resin-coated carrier. A resin-coated carrier of relatively high specific volume resistance was prepared by changing the coating amount of silicone resin, while by changing the addition amount (internal addition and external addition) of carbon black (#600 manufactured by Mitsubishi Chemical Industries) as the electrically conductive particle to attain a relatively low specific volume resistance.
The magnetic toner and the resin-coated magnetic carrier thus produce was mixed in a predetermined ratio to prepare magnetic developers of different toner concentrations.
The developing properties of each of the magnetic developers were tested by continuous development of 1000 sheets of A4 size papers. The operating conditions employed were as follows. Initially, the OPC surface of the photoconductive drum 3 rotating clockwise at a peripheral speed of 30 mm/sec was uniformly charged to -700 V. The permanent magnet member 4, which was formed from a 16-pole ferrite magnet (YBM-3 manufactured by Hitachi Metals, Ltd.) having 20 mm outer diameter and 500 G of surface magnetic flux density, was rotated counterclockwise at a peripheral speed of 147 mm/sec. The developing gap (g) and the doctor gap (t) were 0.4 mm and 0.3 mm respectively. The magnetic developer on the permanent magnet member 4 was biased to -550 V with direct current through the doctor blade 5.
The charging brush 6 was formed by setting a plurality of carbon fiber bristles having a specific volume resistance of 105 Ω·cm into a substrate of SUS304. The length of bristles was 10 min. The transfer roll 7 having an outer diameter of 20 mm was produced by coating around a shaft made Of SUS304 with an ethylene-propylene rubber layer having a hardness (Hs) of 80° and a thickness of 2 mm and pressed against the photoconductive drum 3.
The results of the test are shown in Table 1.
TABLE 1
__________________________________________________________________________
Specific Toner
Volume Amount
Amount of Carbon Black
Concen- Back-
Test
Resistance
of Resin
internally
externally
tration
Image
ground
Carrier
No.
(Ω · cm)
(wt parts)*.sup.1
(wt %)*.sup.2
(wt parts)*.sup.3
(wt %)
Density
Fogging
Adhesion
__________________________________________________________________________
1*.sup.4
3 × 10.sup.3
3 20 2 20 1.42
0.35
occurred
2 4 × 10.sup.5
3 10 2 20 1.40
0.08
none
3 6 × 10.sup.7
0.5 0 0 20 1.39
0.08
none
4 .sup. 4 × 10.sup.10
1.5 0 0 20 1.37
0.10
none
5*.sup.4
.sup. 3 × 10.sup.11
2.0 0 0 20 1.01
0.08
none
6 6 × 10.sup.7
0.5 0 0 10 1.29
0.07
none
7 6 × 10.sup.7
0.5 0 0 40 1.38
0.08
none
8 6 × 10.sup.7
0.5 0 0 60 1.39
0.08
none
9 6 × 10.sup.7
0.5 0 0 80 1.42
0.10
none
__________________________________________________________________________
Note:
*.sup.1 Weight parts of the resin base on 100 weight parts of the carrier
core.
*.sup.2 Weight percent of carbon black based on the resin layer.
*.sup.3 Weight parts of carbon black based on 100 weight parts of the
carrier.
*.sup.4 Comparative Example.
As seen from Table 1, in Test No. 1, the carrier adhered to the photoconductive drum due to a low specific volume resistance, while the image density was low in Test No. 5 due to a high specific volume resistance. In the inventive examples (Test Nos. 2-4 and 6-9), images of high quality were obtained without any defects occurred in Test Nos. 1 and 5. Further, as seen from Test Nos. 6-9, the method of the present invention provided high-quality images over a wide toner concentration range from 10 to 80 weight %.
A non-magnetic toner having an average particle size of 8.5 μm and a particle size distribution of 3-15 μm was prepared in the same manner as in Example 1 except for using the following starting mixture.
87 weight parts of polyester resin (KTR2150 manufactured by Kao Corporation),
10 weight parts of carbon black (#44 manufactured by Mitsubishi Chemical Corporation),
2 weight parts of polypropylene (TP32 manufactured by Sanyo Chemical Industries, Ltd.), and
1 weight part of a charge-controlling agent (Kaya Charge T2N manufactured by Nippon Kayaku Co., Ltd.).
The non-magnetic toner thus prepared had a volume specific resistance of 5×1014 Ω·cm and a triboelectric charge of -29 μC/g.
As the carrier, flat iron powder having an average particles size of 50 μm, a particle size distribution of 10-70 μm, and a magnetization (ρ1000) of 120 emu/g was used. The carrier was coated with a silicone resin to prepare each resin-coated carrier having a desired specific volume resistance in the same manner as in Example 1.
The image forming tests (continuous development of 1000 sheets of A4 size papers) were carried out under the following operating conditions. Initially, the OPC surface of the photoconductive drum 3 rotating clockwise at a peripheral speed of 30 mm/sec was uniformly charged to -650 V. The permanent magnet member 4, which was formed from a 32-pole ferrite magnet (YBM-3 manufactured by Hitachi Metals, Ltd.) having 20 mm outer diameter and 350 G of surface magnetic flux density, was rotated counterclockwise at a peripheral speed of 74 mm/sec. The developing gap (g) and the doctor gap (t) were 0.4 mm and 0.25 mm, respectively. The magnetic developer on the permanent magnet member 4 was biased to -500 V with direct current through the doctor blade 5. The same charging brush and the transfer roll as employed in Example 1 were used.
The results are shown in Table 2.
TABLE 2
__________________________________________________________________________
Specific Toner
Volume Amount
Amount of Carbon Black
Concen- Back-
Test
Resistance
of Resin
internally
externally
tration
Image
ground
Carrier
No.
(Ω · cm)
(wt parts)*.sup.1
(wt %)*.sup.2
(wt parts)*.sup.3
(wt %)
Density
Fogging
Adhesion
__________________________________________________________________________
10*.sup.4
1 × 10.sup.3
3 20 2 30 1.41
0.35
occurred
11 3 × 10.sup.5
3 10 2 30 1.41
0.11
none
12 7 × 10.sup.8
1.0 0 0 30 1.40
0.10
none
13 .sup. 5 × 10.sup.10
1.5 0 0 30 1.37
0.08
none
14*.sup.4
.sup. 8 × 10.sup.12
2.5 0 0 30 1.13
0.15
none
15 7 × 10.sup.8
1.0 0 0 10 1.30
0.08
none
16 7 × 10.sup.8
1.0 0 0 40 1.40
0.09
none
17 7 × 10.sup.8
1.0 0 0 60 1.42
0.10
none
__________________________________________________________________________
Note:
*.sup.1 Weight parts of the resin base on 100 weight parts of the carrier
core.
*.sup.2 Weight percent of carbon black based on the resin layer.
*.sup.3 Weight parts of carbon black based on 100 weight parts of the
carrier.
*.sup.4 Comparative Example.
As seen from Table 2, in Test No. 10, the carrier adhered to the photoconductive drum due to a low specific volume resistance to produce image of poor quality, while the image density was low in Test No. 14 due to a high specific volume resistance. In the inventive examples (Test Nos. 11-13 and 15-17), images of high quality were obtained without any defects occurred in Test Nos. 11 and 14. Further, as seen from Test Nos. 15-17, the method of the present invention provided high-quality images over a wide toner concentration range from 10 to 60 weight %.
The effects achieved by the construction and function described above will be summarized below.
(1) Since the specific volume resistance of the magnetic carrier is restricted to a particular range to prevent the carrier from adhering to the photoconductive drum, the leak at the charging brush can be effectively avoided, this resulting in reproduction of high-quality images without causing developing defects.
(2) Since a sleeve-less developing roll consisting of only the permanent magnet member is used, the developing unit and the electrophotographic recording apparatus can be miniaturized.
(3) Since directly attracted on the permanent magnet member, the magnetic developer is constantly transported to the developing zone and the shape of magnetic brush on the permanent magnet member is stabilized to improve the developability.
(4) Since a two-component magnetic developer having a wide toner concentration range can be used, a means for regulating the toner concentration is not required, this being advantageous for reducing the size of an image forming apparatus.
Claims (8)
1. A method of electrostatically forming a visual image, comprising the steps of:
charging the surface of a rotating photoconductive drum to a uniform potential by a charging brush;
exposing the charged surface of said photoconductive drum to a light image to form an electrostatic latent image;
forming a visual toner image on said photoconductive drum by developing said electrostatic latent image in a developing zone with a two-component magnetic developer which is transported to said developing zone by a rotating cylindrical permanent magnet member having on the circumferential surface thereof a plurality of magnetic poles extending along the axial direction, said magnetic developer comprising a magnetic carrier having a specific volume resistance of 105 -1010 Ω·cm and a magnetic or non-magnetic toner;
transferring said toner image to a recording sheet by means of a transfer roll having an elastic surface; and
fixing the transferred toner image to said recording sheet, wherein an outer diameter (D) of said permanent magnet, a peripheral speed (Vm) of said permanent magnet member, a number, (M) of magnetic poles on a circumferential surface of said permanent magnet member, and a peripheral speed (Vp) of said photoconductive drum are selected such that (πD·Vp)/(M·Vm) is less than 2 mm.
2. The method according to claim 1, wherein the ratio of the peripheral speed of said permanent magnet member to the peripheral speed of said photoconductive drum is 1-10.
3. The method according to claim 1, wherein said magnetic carrier is coated with a resin layer.
4. The method according to claim 3, wherein said resin layer contains an electrically conductive particle internally added thereto, an electrically conductive particle externally added thereto, or the both.
5. The method according to claim 4, wherein said internally added particle is contained in an amount of 5-15 weight % based on the total amount of said resin layer.
6. The method according to claim 4, wherein said externally added particle is contained in an amount of 0.5-5 weight parts based on 100 weight parts of carrier core.
7. The method according to claim 1, wherein the toner concentration in said magnetic developer containing said magnetic toner is 10-90 weight %.
8. The method according to claim 1, wherein the toner concentration in said magnetic developer containing said non-magnetic toner is 5-60 weight %.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP7078778A JPH08272156A (en) | 1995-04-04 | 1995-04-04 | Image forming method |
| JP7-078778 | 1995-04-04 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US5669051A true US5669051A (en) | 1997-09-16 |
Family
ID=13671362
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US08/627,182 Expired - Fee Related US5669051A (en) | 1995-04-04 | 1996-04-03 | Method of electrostatically forming visual image |
Country Status (2)
| Country | Link |
|---|---|
| US (1) | US5669051A (en) |
| JP (1) | JPH08272156A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20030161666A1 (en) * | 2002-02-25 | 2003-08-28 | Konica Corporation | Image forming apparatus provided with developing device using magnetic brush developing method |
| US10591848B2 (en) * | 2017-12-14 | 2020-03-17 | Konica Minolta, Inc. | Magnet roller, developing roller, developing device, and image forming apparatus |
Citations (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS57130407A (en) * | 1981-02-06 | 1982-08-12 | Daido Steel Co Ltd | Cylindrical anisotropic resin magnet |
| JPS59905A (en) * | 1982-06-26 | 1984-01-06 | Yamauchi Rubber Ind Co Ltd | Magnet roll and its preparation |
| JPS59226367A (en) * | 1983-06-08 | 1984-12-19 | Hitachi Metals Ltd | Production of anisotropic magnet roll |
| JPS62201463A (en) * | 1986-02-28 | 1987-09-05 | Hitachi Metals Ltd | Developing method |
| US5246513A (en) * | 1990-09-26 | 1993-09-21 | Mitsubishi Denki Kabushiki Kaisha | Die bonding apparatus and method of controlling the same |
| JPH0764342A (en) * | 1993-08-24 | 1995-03-10 | Hitachi Metals Ltd | Developing carrier and image forming method using the same |
| US5432033A (en) * | 1993-04-01 | 1995-07-11 | Hitachi Metals, Ltd. | Method of electrophotographically forming visual image |
| US5554477A (en) * | 1992-06-15 | 1996-09-10 | Kyocera Corporation | Developer for developing latent electrostatic images |
-
1995
- 1995-04-04 JP JP7078778A patent/JPH08272156A/en active Pending
-
1996
- 1996-04-03 US US08/627,182 patent/US5669051A/en not_active Expired - Fee Related
Patent Citations (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS57130407A (en) * | 1981-02-06 | 1982-08-12 | Daido Steel Co Ltd | Cylindrical anisotropic resin magnet |
| JPS59905A (en) * | 1982-06-26 | 1984-01-06 | Yamauchi Rubber Ind Co Ltd | Magnet roll and its preparation |
| JPS59226367A (en) * | 1983-06-08 | 1984-12-19 | Hitachi Metals Ltd | Production of anisotropic magnet roll |
| JPS62201463A (en) * | 1986-02-28 | 1987-09-05 | Hitachi Metals Ltd | Developing method |
| US5246513A (en) * | 1990-09-26 | 1993-09-21 | Mitsubishi Denki Kabushiki Kaisha | Die bonding apparatus and method of controlling the same |
| US5554477A (en) * | 1992-06-15 | 1996-09-10 | Kyocera Corporation | Developer for developing latent electrostatic images |
| US5432033A (en) * | 1993-04-01 | 1995-07-11 | Hitachi Metals, Ltd. | Method of electrophotographically forming visual image |
| JPH0764342A (en) * | 1993-08-24 | 1995-03-10 | Hitachi Metals Ltd | Developing carrier and image forming method using the same |
| US5483329A (en) * | 1993-08-24 | 1996-01-09 | Hitachi Metals, Ltd. | Carrier for developer and method of electrophotographically forming visual image using same |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20030161666A1 (en) * | 2002-02-25 | 2003-08-28 | Konica Corporation | Image forming apparatus provided with developing device using magnetic brush developing method |
| EP1338926A3 (en) * | 2002-02-25 | 2005-04-13 | Konica Corporation | Image forming apparatus provided with developing device using magnetic brush developing method |
| US10591848B2 (en) * | 2017-12-14 | 2020-03-17 | Konica Minolta, Inc. | Magnet roller, developing roller, developing device, and image forming apparatus |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH08272156A (en) | 1996-10-18 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US5659852A (en) | Image forming method, image forming apparatus and process cartridge | |
| JPH06289689A (en) | Image forming method | |
| JP3812955B2 (en) | Carrier for developer and image forming method using the same | |
| US5374978A (en) | Developing method | |
| US4666815A (en) | Method for developing electrostatic latent image with non-magnetic toner | |
| US5866289A (en) | Developer for electrostatic development and electrostatic developing method using same | |
| US5669051A (en) | Method of electrostatically forming visual image | |
| JPH0611951A (en) | Electrophotographic printer | |
| US5554479A (en) | Image formation method | |
| US6134413A (en) | Carrier for magnetic developer and method of electrophotographically forming visual image | |
| US5516613A (en) | Binary developer | |
| US5565967A (en) | Method of forming image using magnetic developer with high volume resistivity | |
| US5634182A (en) | Method of developing electrostatic latent image | |
| JPH0830078A (en) | Image forming method | |
| JPH086305A (en) | Magnetic carrier for developer | |
| JPH09325611A (en) | Image forming method | |
| JP3198364B2 (en) | Charging method | |
| JP3384106B2 (en) | Development method | |
| JP3087934B2 (en) | Photoconductor charging device | |
| JP3422107B2 (en) | Development method | |
| JPH06332266A (en) | Developing device | |
| JPH05150667A (en) | Developing device | |
| JPS59210466A (en) | Developing method of electrostatic charged image | |
| JPH07234588A (en) | Image forming method | |
| JPH0836291A (en) | Image forming device |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| AS | Assignment |
Owner name: HITACHI METALS, LTD., JAPAN Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:OCHIAI, MASAHISA;SAITOH, TSUTOMU;ASANAE, MASUMI;REEL/FRAME:008004/0220 Effective date: 19960607 |
|
| FEPP | Fee payment procedure |
Free format text: PAYOR NUMBER ASSIGNED (ORIGINAL EVENT CODE: ASPN); ENTITY STATUS OF PATENT OWNER: LARGE ENTITY |
|
| FPAY | Fee payment |
Year of fee payment: 4 |
|
| REMI | Maintenance fee reminder mailed | ||
| LAPS | Lapse for failure to pay maintenance fees | ||
| STCH | Information on status: patent discontinuation |
Free format text: PATENT EXPIRED DUE TO NONPAYMENT OF MAINTENANCE FEES UNDER 37 CFR 1.362 |
|
| FP | Lapsed due to failure to pay maintenance fee |
Effective date: 20050916 |